Glycine cleavage system H protein, mitochondrial (GCSH)

Homo sapiens — UniProt P23434

Gene: GCSHHomo sapiensSwissProt reviewed

About Glycine cleavage system H protein, mitochondrial

Glycine cleavage system H protein, mitochondrial (GCSH) is a protein from Homo sapiens identified by UniProt accession P23434, 173 residues long. MolForge cross-references it against 0 known binders and 133 disease associations.

Target properties

Protein nameGlycine cleavage system H protein, mitochondrial
UniProt accessionP23434
GeneGCSH
OrganismHomo sapiens
Length173 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (133)

Diseases linked to this target (Open Targets).

  • glycine encephalopathy · score 0.71
  • glycine measurement · score 0.50
  • neurodegenerative disease · score 0.48
  • infantile glycine encephalopathy · score 0.37
  • atypical glycine encephalopathy · score 0.37
  • neonatal glycine encephalopathy · score 0.37
  • serum metabolite measurement · score 0.31
  • lysosomal storage disease · score 0.22
  • genetic disorder · score 0.19
  • Myopia · score 0.18

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-P23434-F1alphafoldPREDICTED85.02—

Amino-acid sequence (173 residues)

MALRVVRSVR ALLCTLRAVP SPAAPCPPRP WQLGVGAVRT LRTGPALLSV RKFTEKHEWV TTENGIGTVG ISNFAQEALG DVVYCSLPEV GTKLNKQDEF GALESVKAAS ELYSPLSGEV TEINEALAEN PGLVNKSCYE DGWLIKMTLS NPSELDELMS EEAYEKYIKS IEE

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Quick facts

UniProtP23434
GeneGCSH
OrganismHomo sapiens
Length173
Binders0
Diseases133
View on UniProt